Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs730882026 0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs869025608 0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 20
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24